US20070196594A1 - Photo-alignment material and liquid crystal display device and its manufacturing method using the same - Google Patents

Photo-alignment material and liquid crystal display device and its manufacturing method using the same Download PDF

Info

Publication number
US20070196594A1
US20070196594A1 US11/785,733 US78573307A US2007196594A1 US 20070196594 A1 US20070196594 A1 US 20070196594A1 US 78573307 A US78573307 A US 78573307A US 2007196594 A1 US2007196594 A1 US 2007196594A1
Authority
US
United States
Prior art keywords
photo
alignment
group
liquid crystal
alignment material
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
US11/785,733
Other versions
US8491973B2 (en
Inventor
Mi Nam
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
LG Display Co Ltd
Original Assignee
LG Philips LCD Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by LG Philips LCD Co Ltd filed Critical LG Philips LCD Co Ltd
Priority to US11/785,733 priority Critical patent/US8491973B2/en
Assigned to LG.PHILLIPS LCD. CO., LTD. reassignment LG.PHILLIPS LCD. CO., LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: NAM, MI SOOK
Publication of US20070196594A1 publication Critical patent/US20070196594A1/en
Assigned to LG DISPLAY CO., LTD. reassignment LG DISPLAY CO., LTD. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: LG.PHILIPS LCD CO., LTD.
Application granted granted Critical
Publication of US8491973B2 publication Critical patent/US8491973B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/02Polyamines
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods
    • G02F1/1337Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods
    • G02F1/1337Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
    • G02F1/133711Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by organic films, e.g. polymeric films
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • G03F7/038Macromolecular compounds which are rendered insoluble or differentially wettable
    • G03F7/0384Macromolecular compounds which are rendered insoluble or differentially wettable with ethylenic or acetylenic bands in the main chain of the photopolymer
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2323/00Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2323/00Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
    • C09K2323/02Alignment layer characterised by chemical composition
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2323/00Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
    • C09K2323/02Alignment layer characterised by chemical composition
    • C09K2323/021Inorganic, e.g. glass or silicon oxide
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2323/00Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
    • C09K2323/02Alignment layer characterised by chemical composition
    • C09K2323/025Polyamide
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2323/00Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
    • C09K2323/02Alignment layer characterised by chemical composition
    • C09K2323/027Polyimide
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2323/00Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
    • C09K2323/03Viewing layer characterised by chemical composition
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods
    • G02F1/1337Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
    • G02F1/13378Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by treatment of the surface, e.g. embossing, rubbing or light irradiation
    • G02F1/133788Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by treatment of the surface, e.g. embossing, rubbing or light irradiation by light irradiation, e.g. linearly polarised light photo-polymerisation

Definitions

  • the present invention relates to alignment layers for liquid crystal display devices (hereinafter abbreviated LCD). More particularly, it relates to a photo-alignment material having a photo-reactive functional group of ethenyl at a main-chain, and to the use of that material in liquid crystal displays.
  • LCD liquid crystal display devices
  • Flat panel LCD devices have become widely used as displays for mobile terminals, notebook computers, office equipment, video equipment, and the like. This is because flat panel LCD devices have advantages of small-size, lightweight, and low power consumption.
  • an LCD includes a pair of substrates that are separated by a predetermined interval, and an interposed liquid crystal.
  • An LCD has numerous functional requirements, including light transmission characteristics, operational response time, viewing angle, and contrast. Many of those requirements are impacted by the alignment characteristics of the liquid crystal molecules in the LCD. Indeed, uniformly aligned liquid crystal molecules are important to the electro-optical characteristics of LCDs.
  • the alignment characteristics of LCDs are results of an alignment layer.
  • a rubbing technique has been used to form that layer.
  • a special cloth is rubbed over a substrate to form the alignment layer.
  • the rubbing technique is a simple process, it has problems. For example, various process variables related to rubbing are difficult to accurately control. Furthermore, dust adsorption, unwanted scratches generated by the rubbing, and damage to thin film transistors caused by static electricity can also result from the rubbing. Such problems reduce the manufacturing yield and the performance of LCDs.
  • Photo-alignment methods include photo-decomposition, photo-polymerization, and photo-isomerization. In these methods, optical anisotropy is brought about in a polymer layer by inducing a photo-reaction after most of the molecules facing a polarizing direction in the disorderly-aligned polymer molecules have absorbed light.
  • liquid crystals are arranged by inducing optical anisotropy using a photo-decomposition reaction that selectively breaks partial bonds of the molecules in a specific direction by the application of linearly-polarized ultraviolet rays to a polymer layer consisting of a photo-alignment material.
  • the material typically used for this method is polyimide.
  • polyimide requires the application of ultraviolet rays for a relatively long time to induce liquid crystal alignment
  • a polyimide alignment layer formed by photo-decomposition has a relatively-high thermal stability as compared to other photo-alignment layers fabricated by other methods.
  • liquid crystals are arranged by polymerizing the molecules in a specific direction by applying linearly-polarized rays to a polymer layer where polymerization is to occur.
  • cis/trans isomers are formed by a polarized light.
  • liquid crystals are aligned by the direction generated from the transformation of the produced isomers.
  • the alignment direction is reversibly controlled by applying light of a specific wave length, it is difficult to give a pre-tilt angle to a liquid crystal as well as to maintain the stability of the liquid crystal.
  • the chemical structure of photo-alignment materials is mainly divided into two categories: a main chain, and side chains including photo-sensitive groups such as an alkyl group, an ethenyl group and the like.
  • the main chain makes liquid crystal molecules arrange to face a predetermined direction, while the side chains form a pre-tilt angle.
  • Photo-reactions take place at side chains having photosensitive groups when light is irradiated onto them.
  • liquid crystal alignment depends on the side chains. Therefore, liquid crystal alignment of the photo-alignment material is controlled by the side chains, which include hydrocarbon branches such as alkyl, ethenyl and the like.
  • the photo-alignment of a photo-alignment layer according to the related art is controlled by the side chains.
  • the side chains are flexible and fragile, that alignment tends to be easily broken by thermal, physical, electrical, and photo shocks.
  • the alignment tends to be hard to restore.
  • the photo-alignment layer used in the photo-decomposition method has such poor photo-sensitivity that relatively high light intensity is required to break the predetermined bonds of the side chain or main chain.
  • the actual liquid crystal alignment is relatively poor.
  • the present invention is directed to a photo-alignment material, to a liquid crystal display device that incorporates that photo-alignment material, and to a method of manufacturing a liquid crystal display device that incorporates that photo-alignment material, wherein that photo-alignment material substantially obviates one or more of the problems due to limitations and disadvantages of the related art.
  • a photo-alignment material according to the present invention includes at least a photo-reactive ethenyl functional group at a polymer main chain.
  • a liquid crystal display device in accord with the principles of the present invention includes a first substrate, a second substrate, a liquid crystal layer between the first and second substrates, and a photo-alignment layer on the first and/or the second substrate.
  • That photo-alignment layer includes an ethenyl group on a main chain of the photo-alignment material.
  • a method of fabricating a liquid crystal display device includes preparing a first substrate and a second substrate, forming a photo-alignment layer having an ethenyl group at a main chain on at least the first substrate; and forming a liquid crystal layer between the first and second substrates.
  • FIG. 1 shows a cross-sectional view of a general liquid crystal display device.
  • a liquid crystal display device includes a first substrate, a second substrate, a liquid crystal layer formed between the first and second substrates, and a photo-alignment layer formed at least on the first substrate, wherein the photo-alignment layer is formed from a photo-alignment material having an ethenyl group in a main chain.
  • the alignment stability with respect to thermal, physical, electrical, and photo shocks is increased by that photo-alignment layer.
  • a photo-alignment material according to the present invention consists of polymers denoted by the following Chemical Formula 1.
  • Components ‘A’, ‘B’, and ‘C’ are monomers constituting the polymer and are selectively coupled to produce a homopolymer, a copolymer, or a block-copolymer.
  • the arrangement order of components ‘A’, ‘B’, and ‘C’ is not limited by the above Chemical Formula 1.
  • subscripts ‘a’, ‘b’, and ‘c’ denote component ratios between the respective monomers, where 0 ⁇ a ⁇ 1, 0 ⁇ b ⁇ 1, and 0 ⁇ c ⁇ 1.
  • Component ‘A’ is a monomer including a photo-reactive ethenyl group. That component is selected from groups designated in the following Chemical Formula 2, substituted-structure groups of Chemical Formula 2 with a halogen, a cyano, a nitro, an amino group and the like, and other substituted-structure groups with an alkyl, a haloalkyl, or a cyanoalkyl group having 1 to 10 cartons, or an aryl, an alkylaryl, a haloaryl, a haloalkyl aryl, a nitroaryl, or a cyanoaryl group having 3 to 8 carbons.
  • Components ‘B’ and ‘C’ are selected independently from the following groups shown in Chemical Formula 3, substituted-structure groups of Chemical Formula 3 with a halogen, a cyano, a nitro, an amino group and the like, and other substituted-structure groups with carbonated groups of which carbon number n lies between 1 and 10 such as an alkyl, a haloalkyl, and a cyanoalkyl or other carbonated groups of which carbon number lies between 3 and 8 such as an alkylaryl, a haloaryl, a nitroaryl, a cyanoaryl and the like.
  • Components ‘B’ and ‘C’ which are non-photosensitive components connected to component ‘A’ regardless of a photo-reactive ethenyl group of the present invention, increase the reaction of the photo-sensitive ethenyl groups, secures a marginal space for the reaction, or increases the reciprocal reaction with liquid crystals.
  • a photo-alignment material according to the principles of the present invention is formed by connecting other main chains to a main chain including a photo-reactive ethenyl group.
  • the photo-alignment material described above provides a photo-alignment layer in which photo-reactivity and alignment stability are improved.
  • a liquid crystal display device using the photo-alignment material according to the present invention is explained with reference to FIG. 1 , which shows a cross-sectional view of a liquid crystal display device.
  • a liquid crystal display device according to the principles of the present invention includes a first substrate 1 , a second substrate 2 , a liquid crystal layer 3 formed between the first and second substrates, and a spacer 20 that maintains a uniform interval between the substrates 1 and 2 .
  • the first substrate 1 is a substrate for thin film transistor (hereinafter abbreviated TFT) switching devices that selectively turn data signals on/off in accordance with gate voltages.
  • TFT thin film transistor
  • the first substrate 1 is a gate line having a gate electrode 11 for a thin film transistor and a gate insulating layer 12 over the substrate and the gate electrode 11 .
  • the gate insulating layer is beneficially a silicon nitride layer (SiNx).
  • a semiconductor layer 13 is on the gate insulating layer 12 and over the gate electrode 11 .
  • a data line 14 crosses the gate line.
  • a source electrode 14 a and a drain electrode 14 b are on the semiconductor layer 13 .
  • a first passivation layer 15 is formed over the substrate as shown in FIG.
  • the first passivation layer 15 is beneficially of silicon nitride (SiNx) or BCB (Benzocyclo Butene).
  • a pixel electrode 8 that connects to the drain electrode 14 b is formed on the first passivation layer 15 .
  • the pixel electrode 8 is beneficially of ITO (indium tin oxide).
  • a first alignment layer 4 a extends over the surface, including the pixel electrode 8 , as shown in FIG. 1 .
  • the second substrate 2 supports a color filter layer for expressing colors.
  • black matrices 16 that prevents light leakage
  • a color filter layer 17 (RGB) between neighboring black matrices 16
  • a second passivation layer 18 over the entire surface as shown in FIG. 1 .
  • the second passivation layer 18 protects the color filter layer 17 .
  • a common electrode 19 is then formed on the second passivation layer 18 .
  • the common electrode 19 is beneficially comprised of ITO (indium-tin-oxide).
  • a second alignment layer 4 b is then formed over the entire surface as shown in FIG. 1 .
  • At least one of the first and second alignment layers 4 a and 4 b is formed from a photo-alignment material that is in accord with the principles of the present invention. If the other alignment layer is not formed from a photo-alignment layer material, it can be formed by rubbing.
  • the photo-alignment material is uniformly coated on a substrate. That photo-alignment layer material is then thermally treated and dried in an oven. Subsequently, a structure that assists anisotropy of the liquid crystals is attained by irradiating polarized UV rays onto the exposed surface of the photo-alignment layer.
  • the UV rays may be irradiated vertically and slantwise using unpolarized light, non-polarized light, linearly polarized light, partially polarized light or the like, depending on the alignment structure to be implemented.
  • a photo-alignment layer according to the present invention enables improvement of the optical and thermal stability of the liquid crystal alignment, pre-tilt stability against electric stress, and improved shock-resistance. Moreover, the principles of the present invention enable improved display quality and an improved LCD display manufacturing method.

Abstract

A photo-alignment material, a liquid crystal display device using the photo-alignment material, and a manufacturing method. The photo-alignment material is a polymer having a photo-reactive ethenyl group on a main chain. When used as a photo-alignment layer, the photo-alignment material enables improved alignment stability against external shocks, light, and heat. The liquid crystal display device includes a first substrate, a second substrate, a liquid crystal layer formed between the first and second substrates, and a photo-alignment layer formed at least on the first substrate, with the photo-alignment layer formed from a photo-alignment material having an ethenyl group at a main chain.

Description

    BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • The present invention relates to alignment layers for liquid crystal display devices (hereinafter abbreviated LCD). More particularly, it relates to a photo-alignment material having a photo-reactive functional group of ethenyl at a main-chain, and to the use of that material in liquid crystal displays.
  • 2. Background of the Related Art
  • Flat panel LCD devices have become widely used as displays for mobile terminals, notebook computers, office equipment, video equipment, and the like. This is because flat panel LCD devices have advantages of small-size, lightweight, and low power consumption.
  • In general, an LCD includes a pair of substrates that are separated by a predetermined interval, and an interposed liquid crystal.
  • An LCD has numerous functional requirements, including light transmission characteristics, operational response time, viewing angle, and contrast. Many of those requirements are impacted by the alignment characteristics of the liquid crystal molecules in the LCD. Indeed, uniformly aligned liquid crystal molecules are important to the electro-optical characteristics of LCDs.
  • The alignment characteristics of LCDs are results of an alignment layer. Generally, a rubbing technique has been used to form that layer. In that technique, a special cloth is rubbed over a substrate to form the alignment layer. While the rubbing technique is a simple process, it has problems. For example, various process variables related to rubbing are difficult to accurately control. Furthermore, dust adsorption, unwanted scratches generated by the rubbing, and damage to thin film transistors caused by static electricity can also result from the rubbing. Such problems reduce the manufacturing yield and the performance of LCDs.
  • Because of the forgoing problems, significant effort has been expended in developing alignment techniques that do not use mechanical rubbing. In particular, photo-alignment methods could solve the static electricity and dust problems, as well as improve the viewing angle.
  • Photo-alignment methods include photo-decomposition, photo-polymerization, and photo-isomerization. In these methods, optical anisotropy is brought about in a polymer layer by inducing a photo-reaction after most of the molecules facing a polarizing direction in the disorderly-aligned polymer molecules have absorbed light.
  • In the photo-decomposition method, liquid crystals are arranged by inducing optical anisotropy using a photo-decomposition reaction that selectively breaks partial bonds of the molecules in a specific direction by the application of linearly-polarized ultraviolet rays to a polymer layer consisting of a photo-alignment material. The material typically used for this method is polyimide. Although polyimide requires the application of ultraviolet rays for a relatively long time to induce liquid crystal alignment, a polyimide alignment layer formed by photo-decomposition has a relatively-high thermal stability as compared to other photo-alignment layers fabricated by other methods.
  • In the photo-polymerization method, liquid crystals are arranged by polymerizing the molecules in a specific direction by applying linearly-polarized rays to a polymer layer where polymerization is to occur.
  • In the photo-isomerization method, cis/trans isomers are formed by a polarized light. Thus, liquid crystals are aligned by the direction generated from the transformation of the produced isomers. Although the alignment direction is reversibly controlled by applying light of a specific wave length, it is difficult to give a pre-tilt angle to a liquid crystal as well as to maintain the stability of the liquid crystal.
  • The chemical structure of photo-alignment materials is mainly divided into two categories: a main chain, and side chains including photo-sensitive groups such as an alkyl group, an ethenyl group and the like. The main chain makes liquid crystal molecules arrange to face a predetermined direction, while the side chains form a pre-tilt angle.
  • Photo-reactions take place at side chains having photosensitive groups when light is irradiated onto them. Thus, liquid crystal alignment depends on the side chains. Therefore, liquid crystal alignment of the photo-alignment material is controlled by the side chains, which include hydrocarbon branches such as alkyl, ethenyl and the like.
  • Unfortunately, related art photo-alignment materials, and LCDs using the same, have problems. As noted, the photo-alignment of a photo-alignment layer according to the related art is controlled by the side chains. As the side chains are flexible and fragile, that alignment tends to be easily broken by thermal, physical, electrical, and photo shocks. Furthermore, the alignment tends to be hard to restore. Additionally, the photo-alignment layer used in the photo-decomposition method has such poor photo-sensitivity that relatively high light intensity is required to break the predetermined bonds of the side chain or main chain. Finally, in general, with related art photo-alignment layers the actual liquid crystal alignment is relatively poor.
  • SUMMARY OF THE INVENTION
  • Accordingly, the present invention is directed to a photo-alignment material, to a liquid crystal display device that incorporates that photo-alignment material, and to a method of manufacturing a liquid crystal display device that incorporates that photo-alignment material, wherein that photo-alignment material substantially obviates one or more of the problems due to limitations and disadvantages of the related art.
  • Additional features and advantages of the invention will be set forth in the description that follows, and in part will be apparent from the description, or may be learned by practice of the invention. The objectives and other advantages of the invention will be realized and attained by the structure particularly pointed out in the written description and claims hereof as well as the appended drawings.
  • To achieve these and other advantages, and in accord with the principles of the present invention as embodied and broadly described, a photo-alignment material according to the present invention includes at least a photo-reactive ethenyl functional group at a polymer main chain.
  • In another aspect, a liquid crystal display device in accord with the principles of the present invention includes a first substrate, a second substrate, a liquid crystal layer between the first and second substrates, and a photo-alignment layer on the first and/or the second substrate. That photo-alignment layer includes an ethenyl group on a main chain of the photo-alignment material.
  • In another aspect, a method of fabricating a liquid crystal display device according to the principles of the present invention includes preparing a first substrate and a second substrate, forming a photo-alignment layer having an ethenyl group at a main chain on at least the first substrate; and forming a liquid crystal layer between the first and second substrates.
  • It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory and are intended to provide further explanation of the invention as claimed.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • The accompanying FIG. 1, which is included to provide a further, understanding of the invention and which is incorporated in and constitutes a part of this specification, illustrates an embodiment of the invention and together with the description serves to explain the principles of the invention. Specifically, FIG. 1 shows a cross-sectional view of a general liquid crystal display device.
  • DETAILED DESCRIPTION OF AN ILLUSTRATED EMBODIMENTS
  • Reference will be made in detail to an illustrated preferred embodiment of the present invention, the example of which is illustrated in the accompanying drawing. In the illustrated embodiment a liquid crystal display device includes a first substrate, a second substrate, a liquid crystal layer formed between the first and second substrates, and a photo-alignment layer formed at least on the first substrate, wherein the photo-alignment layer is formed from a photo-alignment material having an ethenyl group in a main chain. The alignment stability with respect to thermal, physical, electrical, and photo shocks is increased by that photo-alignment layer. More specifically, a photo-alignment material according to the present invention consists of polymers denoted by the following Chemical Formula 1.
    Figure US20070196594A1-20070823-C00001
  • Components ‘A’, ‘B’, and ‘C’ are monomers constituting the polymer and are selectively coupled to produce a homopolymer, a copolymer, or a block-copolymer. The arrangement order of components ‘A’, ‘B’, and ‘C’ is not limited by the above Chemical Formula 1. Furthermore, subscripts ‘a’, ‘b’, and ‘c’ denote component ratios between the respective monomers, where 0<a≦1, 0≦b<1, and 0≦c<1.
  • Component ‘A’ is a monomer including a photo-reactive ethenyl group. That component is selected from groups designated in the following Chemical Formula 2, substituted-structure groups of Chemical Formula 2 with a halogen, a cyano, a nitro, an amino group and the like, and other substituted-structure groups with an alkyl, a haloalkyl, or a cyanoalkyl group having 1 to 10 cartons, or an aryl, an alkylaryl, a haloaryl, a haloalkyl aryl, a nitroaryl, or a cyanoaryl group having 3 to 8 carbons.
    Figure US20070196594A1-20070823-C00002
    Figure US20070196594A1-20070823-C00003
    Figure US20070196594A1-20070823-C00004

    Components ‘B’ and ‘C’ are selected independently from the following groups shown in Chemical Formula 3, substituted-structure groups of Chemical Formula 3 with a halogen, a cyano, a nitro, an amino group and the like, and other substituted-structure groups with carbonated groups of which carbon number n lies between 1 and 10 such as an alkyl, a haloalkyl, and a cyanoalkyl or other carbonated groups of which carbon number lies between 3 and 8 such as an alkylaryl, a haloaryl, a nitroaryl, a cyanoaryl and the like.
    Figure US20070196594A1-20070823-C00005
  • Components ‘B’ and ‘C’, which are non-photosensitive components connected to component ‘A’ regardless of a photo-reactive ethenyl group of the present invention, increase the reaction of the photo-sensitive ethenyl groups, secures a marginal space for the reaction, or increases the reciprocal reaction with liquid crystals.
  • Therefore, a photo-alignment material according to the principles of the present invention is formed by connecting other main chains to a main chain including a photo-reactive ethenyl group.
  • The photo-alignment material described above provides a photo-alignment layer in which photo-reactivity and alignment stability are improved.
  • A liquid crystal display device using the photo-alignment material according to the present invention is explained with reference to FIG. 1, which shows a cross-sectional view of a liquid crystal display device. Referring to FIG. 1, a liquid crystal display device according to the principles of the present invention includes a first substrate 1, a second substrate 2, a liquid crystal layer 3 formed between the first and second substrates, and a spacer 20 that maintains a uniform interval between the substrates 1 and 2.
  • The first substrate 1 is a substrate for thin film transistor (hereinafter abbreviated TFT) switching devices that selectively turn data signals on/off in accordance with gate voltages. To that end, on the first substrate 1 are a gate line having a gate electrode 11 for a thin film transistor and a gate insulating layer 12 over the substrate and the gate electrode 11. The gate insulating layer is beneficially a silicon nitride layer (SiNx). A semiconductor layer 13 is on the gate insulating layer 12 and over the gate electrode 11. A data line 14 crosses the gate line. A source electrode 14 a and a drain electrode 14 b are on the semiconductor layer 13. A first passivation layer 15 is formed over the substrate as shown in FIG. 1, including over the source electrode 14 a and the drain electrode 14 b. The first passivation layer 15 is beneficially of silicon nitride (SiNx) or BCB (Benzocyclo Butene). A pixel electrode 8 that connects to the drain electrode 14 b is formed on the first passivation layer 15. The pixel electrode 8 is beneficially of ITO (indium tin oxide). Furthermore, a first alignment layer 4 a extends over the surface, including the pixel electrode 8, as shown in FIG. 1.
  • The second substrate 2 supports a color filter layer for expressing colors. On the second substrate 2 are black matrices 16 that prevents light leakage, a color filter layer 17 (RGB) between neighboring black matrices 16, and a second passivation layer 18 over the entire surface as shown in FIG. 1. The second passivation layer 18 protects the color filter layer 17. A common electrode 19 is then formed on the second passivation layer 18. The common electrode 19 is beneficially comprised of ITO (indium-tin-oxide). A second alignment layer 4 b is then formed over the entire surface as shown in FIG. 1.
  • At least one of the first and second alignment layers 4 a and 4 b is formed from a photo-alignment material that is in accord with the principles of the present invention. If the other alignment layer is not formed from a photo-alignment layer material, it can be formed by rubbing.
  • To form a photo-alignment layer using a photo-alignment material as described above (having an ethenyl group in the main chain), the photo-alignment material is uniformly coated on a substrate. That photo-alignment layer material is then thermally treated and dried in an oven. Subsequently, a structure that assists anisotropy of the liquid crystals is attained by irradiating polarized UV rays onto the exposed surface of the photo-alignment layer. The UV rays may be irradiated vertically and slantwise using unpolarized light, non-polarized light, linearly polarized light, partially polarized light or the like, depending on the alignment structure to be implemented.
  • A photo-alignment layer according to the present invention enables improvement of the optical and thermal stability of the liquid crystal alignment, pre-tilt stability against electric stress, and improved shock-resistance. Moreover, the principles of the present invention enable improved display quality and an improved LCD display manufacturing method.
  • The foregoing embodiments are merely exemplary and are not to be construed as limiting the present invention. The present inventions can be readily applied to other types of apparatuses. The description of the present invention is intended to be illustrative, and not to limit the scope of the claims. Many alternatives, modifications, and variations will be apparent to those skilled in the art.

Claims (4)

1. A photo-alignment material having a photo-reactive ethenyl group in a polymer main chain, wherein the polymer is in accord with chemical formula 1:
Figure US20070196594A1-20070823-C00006
wherein subscripts a, b, and c denote a component ratio of respective monomers, wherein 0<a≦1, 0≦b<1, and 0≦c<1, and wherein component A is a monomer including a photo-reactive ethenyl group selected from groups designated in chemical formula 2, substituted-structure groups of chemical formula 2 having a halogen, a cyano, a nitro, an amino group, and other substituted-structure groups with an alkyl, a haloalkyl, and a cyanoalkyl group having 1 to 10 carbons, or an aryl, an alkyl, an aryl, a haloaryl, a haloalkyl aryl, a nitroaryl, and a cyanoaryl group having 3 to 8 carbons;
Figure US20070196594A1-20070823-C00007
Figure US20070196594A1-20070823-C00008
Figure US20070196594A1-20070823-C00009
2. The photo-alignment material of claim 1, wherein components B and C are selected independently from groups shown in chemical formula 3, substituted-structure groups of chemical formula 3 with a halogen, a cyano, a nitro, an amino group, other substituted-structure groups with carbonated groups of which carbon number n lies between 1 and 10 such as an alkyl, a haloalkyl, and a cyanoalkyl, and other carbonated groups of which carbon number lies between 3 and 8 such as an alkylaryl, a haloaryl, a haloalkylaryl, a nitroaryl, and a cyanoaryl;
Figure US20070196594A1-20070823-C00010
3-32. (canceled)
33. A photo-alignment material having a photo-reactive ethenyl group in a polymer main chain, wherein the polymer is according to formula 1:
Figure US20070196594A1-20070823-C00011
wherein subscripts a, b, and c denote a component ratio of respective monomers, wherein 0<a≦1, 0≦b<1, and 0≦c<1;
wherein component A is a monomer having the photo-reactive ethenyl group of formula 2, and the monomer having a photo-reactive ethenyl group of formula 2 can be substituted with at least one selected from the group consisting of a halogen, a cyano, a nitro, an amino group, an alkyl, a haloalkyl, a cyanoalkyl group having 1 to 10 carbons, an aryl, an alkyl, a haloaryl, a haloalkyl aryl, a nitroaryl, and a cyanoaryl group having 3 to 8 carbons;
wherein formula 2 is selected from a group consisting of:
Figure US20070196594A1-20070823-C00012
Figure US20070196594A1-20070823-C00013
Figure US20070196594A1-20070823-C00014
wherein component B and C are monomers having a non-photosensitive component of formula 3, and the monomers having a non-photosensitive component of formula 3 can be substituted with at least one selected from the group consisting of a halogen, a cyano, a nitro, an amino group, alkyl, a haloalkyl, a cyanoalkyl, alkylaryl, a haloaryl, a haloalkylaryl a nitroaryl, a cyanoaryl;
wherein formula 3 is selected from a group consisting of:
Figure US20070196594A1-20070823-C00015
US11/785,733 2000-12-05 2007-04-19 Photo-alignment material and liquid crystal display device and its manufacturing method using the same Expired - Lifetime US8491973B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US11/785,733 US8491973B2 (en) 2000-12-05 2007-04-19 Photo-alignment material and liquid crystal display device and its manufacturing method using the same

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
KR1020000073270A KR100685944B1 (en) 2000-12-05 2000-12-05 Photo-alignment Material and Liquid Crystal Display Device fabricated with it
KR2000-73270 2000-12-05
US09/893,977 US6627269B2 (en) 2000-12-05 2001-06-29 Photo-alignment material and liquid crystal display device
US10/630,738 US7220467B2 (en) 2000-12-05 2003-07-31 Photo-alignment material and liquid crystal display device and its manufacturing method using the same
US11/785,733 US8491973B2 (en) 2000-12-05 2007-04-19 Photo-alignment material and liquid crystal display device and its manufacturing method using the same

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US10/630,738 Division US7220467B2 (en) 2000-12-05 2003-07-31 Photo-alignment material and liquid crystal display device and its manufacturing method using the same

Publications (2)

Publication Number Publication Date
US20070196594A1 true US20070196594A1 (en) 2007-08-23
US8491973B2 US8491973B2 (en) 2013-07-23

Family

ID=19702678

Family Applications (4)

Application Number Title Priority Date Filing Date
US09/893,977 Expired - Lifetime US6627269B2 (en) 2000-12-05 2001-06-29 Photo-alignment material and liquid crystal display device
US10/630,781 Expired - Lifetime US6797096B2 (en) 2000-12-05 2003-07-31 Photo-alignment material and liquid crystal display device and its manufacturing method using the same
US10/630,738 Expired - Lifetime US7220467B2 (en) 2000-12-05 2003-07-31 Photo-alignment material and liquid crystal display device and its manufacturing method using the same
US11/785,733 Expired - Lifetime US8491973B2 (en) 2000-12-05 2007-04-19 Photo-alignment material and liquid crystal display device and its manufacturing method using the same

Family Applications Before (3)

Application Number Title Priority Date Filing Date
US09/893,977 Expired - Lifetime US6627269B2 (en) 2000-12-05 2001-06-29 Photo-alignment material and liquid crystal display device
US10/630,781 Expired - Lifetime US6797096B2 (en) 2000-12-05 2003-07-31 Photo-alignment material and liquid crystal display device and its manufacturing method using the same
US10/630,738 Expired - Lifetime US7220467B2 (en) 2000-12-05 2003-07-31 Photo-alignment material and liquid crystal display device and its manufacturing method using the same

Country Status (2)

Country Link
US (4) US6627269B2 (en)
KR (1) KR100685944B1 (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100685944B1 (en) * 2000-12-05 2007-02-23 엘지.필립스 엘시디 주식회사 Photo-alignment Material and Liquid Crystal Display Device fabricated with it
US7563490B2 (en) * 2004-12-06 2009-07-21 Semiconductor Energy Laboratory Co., Ltd. Liquid crystal display device
JP2007071928A (en) * 2005-09-05 2007-03-22 Hitachi Ltd Liquid crystal display device
WO2007032292A1 (en) * 2005-09-15 2007-03-22 Semiconductor Energy Laboratory Co., Ltd. Manufacturing method of liquid crystal display device
KR101666622B1 (en) * 2009-08-26 2016-10-17 삼성디스플레이 주식회사 Photoalignment agent and liquid crystal display device using the same
JP5184492B2 (en) 2009-11-19 2013-04-17 株式会社ジャパンディスプレイイースト Liquid crystal display device and manufacturing method thereof
US20140211140A1 (en) * 2013-01-25 2014-07-31 Shenzhen China Star Optoelectronics Technology Co., Ltd. Alignment Film Material and Corresponding Liquid Crystal Panel
DE102015200488A1 (en) * 2015-01-14 2016-07-14 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Electrically controllable interference color filter and its use
US10816855B2 (en) 2015-10-29 2020-10-27 The Hong Kong University Of Science And Technology Composite photoalignment layer

Citations (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4369291A (en) * 1979-04-28 1983-01-18 Bayer Aktiengesellschaft Polyene/α-olefin copolymers
US4416973A (en) * 1982-01-04 1983-11-22 E. I. Du Pont De Nemours & Co. Radiation-sensitive polyimide precursor composition derived from a diaryl fluoro compound
US4974941A (en) * 1989-03-08 1990-12-04 Hercules Incorporated Process of aligning and realigning liquid crystal media
US4974991A (en) * 1989-06-19 1990-12-04 Seid Mandavi Vehicle speed bump device
US5118538A (en) * 1989-03-05 1992-06-02 Hoechst Aktiengesellschaft Electrically conductive polymers and their use as orienting layer in liquid-crystal switching and display elements
US5239398A (en) * 1990-03-15 1993-08-24 Canon Kabushiki Kaisha Liquid crystal device with phenylenevinylene or phenylene sulfide alignment films having particular high electrical conductivity
US5283265A (en) * 1983-12-08 1994-02-01 Hayakawa Rubber Company Limited Photopolymerizable rubber
US5389998A (en) * 1993-04-08 1995-02-14 Eastman Kodak Company Camera power supply system
US5389698A (en) * 1991-07-26 1995-02-14 Hoffmann-La Roche Inc. Process for making photopolymers having varying molecular orientation using light to orient and polymerize
US5464669A (en) * 1993-09-18 1995-11-07 Goldstar Co., Ltd. Method for forming an orientation film of photopolymer in a liquid crystal display
US5486560A (en) * 1992-12-25 1996-01-23 Kabushiki Kaisha Toyota Chuo Kenkyusho Variable-modulus material
US5538823A (en) * 1993-05-20 1996-07-23 Goldstar Co., Ltd. Liquid crystal device utilizing thermostable polymeric material
US5656340A (en) * 1994-06-28 1997-08-12 Hoechst Aktiengesellschaft Liquid crystal display device
US5705096A (en) * 1995-03-15 1998-01-06 Alps Electric Co., Ltd. UV crosslinking compound, alignment film for LCD component and LCD component
US5824377A (en) * 1995-11-20 1998-10-20 Lg Electronics Inc. Photosensitive material for orientation of liquid crystal device and liquid crystal device thereof
US5928561A (en) * 1995-09-29 1999-07-27 The Secretary Of State For Defence In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland Polymers for liquid crystal alignment
US6184959B1 (en) * 1997-10-24 2001-02-06 Sharp Kabushiki Kaisha Liquid crystal display device having alignment film that provides alignment upon irradiation and manufacturing method the same
US6270938B1 (en) * 2000-06-09 2001-08-07 Kodak Polychrome Graphics Llc Acetal copolymers and use thereof in photosensitive compositions
US6274695B1 (en) * 1997-04-30 2001-08-14 Nissan Chemical Industries, Ltd. Aligning agent for liquid crystal
US6627269B2 (en) * 2000-12-05 2003-09-30 Lg.Philips Lcd Co., Ltd. Photo-alignment material and liquid crystal display device
US6682783B1 (en) * 1997-05-16 2004-01-27 Hitachi, Ltd. Active matrix type liquid crystal display apparatus
US6770335B2 (en) * 2000-10-28 2004-08-03 Lg.Philips Lcd Co., Ltd. Photoalignment materials and liquid crystal display device and method for fabricating the same with said materials

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG50575A1 (en) 1991-07-26 2000-12-19 Rolic Ag Image display device with liquid crystal cell
SG50586A1 (en) 1991-07-26 2000-05-23 Rolic Ag Liquid crystal display cell
FR2682922B1 (en) * 1991-10-23 1996-07-05 Thomson Csf METHOD AND DEVICE FOR BRAKING VEHICLES BY CONTROLLING THE BRAKING TORQUE APPLIED ON A WHEEL.
SG64893A1 (en) 1993-02-17 1999-08-17 Rolic Ag Orientating layers for liquid crystals
JP2773795B2 (en) 1995-05-10 1998-07-09 スタンレー電気株式会社 Manufacturing method of liquid crystal alignment structure and liquid crystal display device
JP2996897B2 (en) 1995-06-22 2000-01-11 インターナショナル・ビジネス・マシーンズ・コーポレイション Liquid crystal alignment control method and apparatus, and liquid crystal display device having alignment film formed by the method
TW353046B (en) * 1997-06-06 1999-02-21 Sumitomo Chemical Co Method for producing phase retarder film
JP3272284B2 (en) * 1997-11-04 2002-04-08 科学技術振興事業団 Poly (substituted biphenylene vinylenes) and process for producing the same
KR100357214B1 (en) * 1999-04-21 2002-10-18 엘지.필립스 엘시디 주식회사 Liquid crystal display device
US8211134B2 (en) 2007-09-29 2012-07-03 Restoration Robotics, Inc. Systems and methods for harvesting, storing, and implanting hair grafts

Patent Citations (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4369291A (en) * 1979-04-28 1983-01-18 Bayer Aktiengesellschaft Polyene/α-olefin copolymers
US4416973A (en) * 1982-01-04 1983-11-22 E. I. Du Pont De Nemours & Co. Radiation-sensitive polyimide precursor composition derived from a diaryl fluoro compound
US5283265A (en) * 1983-12-08 1994-02-01 Hayakawa Rubber Company Limited Photopolymerizable rubber
US5118538A (en) * 1989-03-05 1992-06-02 Hoechst Aktiengesellschaft Electrically conductive polymers and their use as orienting layer in liquid-crystal switching and display elements
US4974941A (en) * 1989-03-08 1990-12-04 Hercules Incorporated Process of aligning and realigning liquid crystal media
US5032009A (en) * 1989-03-08 1991-07-16 Hercules Incorporated Process of aligning and realigning liquid crystal media
US4974991A (en) * 1989-06-19 1990-12-04 Seid Mandavi Vehicle speed bump device
US5239398A (en) * 1990-03-15 1993-08-24 Canon Kabushiki Kaisha Liquid crystal device with phenylenevinylene or phenylene sulfide alignment films having particular high electrical conductivity
US5389698A (en) * 1991-07-26 1995-02-14 Hoffmann-La Roche Inc. Process for making photopolymers having varying molecular orientation using light to orient and polymerize
US5486560A (en) * 1992-12-25 1996-01-23 Kabushiki Kaisha Toyota Chuo Kenkyusho Variable-modulus material
US5389998A (en) * 1993-04-08 1995-02-14 Eastman Kodak Company Camera power supply system
US5538823A (en) * 1993-05-20 1996-07-23 Goldstar Co., Ltd. Liquid crystal device utilizing thermostable polymeric material
US5767994A (en) * 1993-09-18 1998-06-16 Goldstar Co., Ltd. Orientation film of photopolymer in a liquid crystal display and a method of forming the film
US5464669A (en) * 1993-09-18 1995-11-07 Goldstar Co., Ltd. Method for forming an orientation film of photopolymer in a liquid crystal display
US5656340A (en) * 1994-06-28 1997-08-12 Hoechst Aktiengesellschaft Liquid crystal display device
US5705096A (en) * 1995-03-15 1998-01-06 Alps Electric Co., Ltd. UV crosslinking compound, alignment film for LCD component and LCD component
US5928561A (en) * 1995-09-29 1999-07-27 The Secretary Of State For Defence In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland Polymers for liquid crystal alignment
US5998563A (en) * 1995-11-20 1999-12-07 Lg Electronics Inc. Photosensitive material for orientation of liquid crystal device and liquid crystal device thereof
US5824377A (en) * 1995-11-20 1998-10-20 Lg Electronics Inc. Photosensitive material for orientation of liquid crystal device and liquid crystal device thereof
US6274695B1 (en) * 1997-04-30 2001-08-14 Nissan Chemical Industries, Ltd. Aligning agent for liquid crystal
US6682783B1 (en) * 1997-05-16 2004-01-27 Hitachi, Ltd. Active matrix type liquid crystal display apparatus
US6184959B1 (en) * 1997-10-24 2001-02-06 Sharp Kabushiki Kaisha Liquid crystal display device having alignment film that provides alignment upon irradiation and manufacturing method the same
US6270938B1 (en) * 2000-06-09 2001-08-07 Kodak Polychrome Graphics Llc Acetal copolymers and use thereof in photosensitive compositions
US6770335B2 (en) * 2000-10-28 2004-08-03 Lg.Philips Lcd Co., Ltd. Photoalignment materials and liquid crystal display device and method for fabricating the same with said materials
US6627269B2 (en) * 2000-12-05 2003-09-30 Lg.Philips Lcd Co., Ltd. Photo-alignment material and liquid crystal display device
US6797096B2 (en) * 2000-12-05 2004-09-28 Lg.Philips Lcd Co., Ltd. Photo-alignment material and liquid crystal display device and its manufacturing method using the same

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Lefebvre et al "1,3 Cyclohexadiene Polymers. Part 1: Preparation and aromatization of Poly-1,3-cyclohexadiene", Journal of Polymer Sci, Part A, vol. 2 3277-3295 ( February, 1964) *

Also Published As

Publication number Publication date
US6797096B2 (en) 2004-09-28
US7220467B2 (en) 2007-05-22
US20040022963A1 (en) 2004-02-05
US8491973B2 (en) 2013-07-23
US6627269B2 (en) 2003-09-30
US20020071079A1 (en) 2002-06-13
KR100685944B1 (en) 2007-02-23
US20040022964A1 (en) 2004-02-05
KR20020044270A (en) 2002-06-15

Similar Documents

Publication Publication Date Title
US11520186B2 (en) Liquid crystal display and method for manufacturing same
US8491973B2 (en) Photo-alignment material and liquid crystal display device and its manufacturing method using the same
US11391993B2 (en) Liquid crystal display device and manufacturing method thereof
US9470929B2 (en) Liquid crystal display unit and method of manufacturing the same
US7248318B2 (en) Liquid crystal display device and method of producing the same
US9146425B2 (en) Liquid crystal display and method of manufacturing the same
US8456607B2 (en) Manufacturing method of liquid crystal display device
US6027772A (en) Optical alignment composition, alignment layer formed using the same and LCD having the alignment layer
US20110109857A1 (en) Liquid crystal display device
US9465244B2 (en) Liquid crystal display
JPWO2010131392A1 (en) Liquid crystal display
JP4469331B2 (en) Method for forming alignment film of liquid crystal display device
WO2014034517A1 (en) Liquid crystal display device and method for manufacturing same
JP4342168B2 (en) Liquid crystal display device and manufacturing method thereof
JP2007108720A (en) Method of manufacturing liquid crystal display device
US7956968B2 (en) Liquid crystal display device and fabrication method thereof
KR20030022431A (en) Thermal crosslinking Polyimide Based Materials And Method For Fabricating Liquid Crystal Display Device By Said It
KR20040013787A (en) Liquid Crystal Display Panel and Method of Fabricating the same

Legal Events

Date Code Title Description
AS Assignment

Owner name: LG.PHILLIPS LCD. CO., LTD., KOREA, REPUBLIC OF

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:NAM, MI SOOK;REEL/FRAME:019272/0590

Effective date: 20010629

AS Assignment

Owner name: LG DISPLAY CO., LTD., KOREA, REPUBLIC OF

Free format text: CHANGE OF NAME;ASSIGNOR:LG.PHILIPS LCD CO., LTD.;REEL/FRAME:021754/0230

Effective date: 20080304

Owner name: LG DISPLAY CO., LTD.,KOREA, REPUBLIC OF

Free format text: CHANGE OF NAME;ASSIGNOR:LG.PHILIPS LCD CO., LTD.;REEL/FRAME:021754/0230

Effective date: 20080304

STCF Information on status: patent grant

Free format text: PATENTED CASE

FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

FPAY Fee payment

Year of fee payment: 4

MAFP Maintenance fee payment

Free format text: PAYMENT OF MAINTENANCE FEE, 8TH YEAR, LARGE ENTITY (ORIGINAL EVENT CODE: M1552); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

Year of fee payment: 8